2022
DOI: 10.3724/abbs.2022004
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Curcumin ameliorates H<sub>2</sub>O<sub>2</sub>-induced injury through SIRT1-PERK-CHOP pathway in pancreatic beta cells

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Cited by 9 publications
(6 citation statements)
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“…A total of 2 × 10 5 cells per well were inoculated in 6-well plates, and each group of cells was treated following the method described by Cao et al After that, the samples to be stained were fully covered with the appropriate amount of the Hoechst 33258 staining solution. The cells were then incubated at 37 °C and 5% CO 2 for 30 min, and the staining solution was discarded, and the cells were washed three times with PBS before observing them under a fluorescence microscope (Nikon, Eclipse Cl, Japan).…”
Section: Methodsmentioning
confidence: 99%
“…A total of 2 × 10 5 cells per well were inoculated in 6-well plates, and each group of cells was treated following the method described by Cao et al After that, the samples to be stained were fully covered with the appropriate amount of the Hoechst 33258 staining solution. The cells were then incubated at 37 °C and 5% CO 2 for 30 min, and the staining solution was discarded, and the cells were washed three times with PBS before observing them under a fluorescence microscope (Nikon, Eclipse Cl, Japan).…”
Section: Methodsmentioning
confidence: 99%
“…Changes in the cell apoptosis rate were assessed by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay. Briefly, the cells were seeded in six-well plates, treated, and stained with Hoechst 33258 (Beyotime, China, catalog number: C1017) stain, as described in a previous study [ 25 ]. The stained cells were viewed and scored under a fluorescence microscope (IX53, Olympus, Tokyo, Japan).…”
Section: Methodsmentioning
confidence: 99%
“…The SOD (superoxide dismutase) activity of the P. notoginseng leaves was quantified using a WST-8 assay kit (Suzhou Keming Biotechnology Co., Ltd.) following previous reports ( Cao et al., 2022 ). In brief, 0.1 g of leaves and 1 mL of extraction solution are ground into homogenate on ice, and then centrifuged at 8000 g and 4°C for 10 min, taking the supernatant as the extract.…”
Section: Methodsmentioning
confidence: 99%